BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

145 related articles for article (PubMed ID: 9156314)

  • 21. Perfect endings: a review of subtelomeric probes and their use in clinical diagnosis.
    Knight SJ; Flint J
    J Med Genet; 2000 Jun; 37(6):401-9. PubMed ID: 10851249
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Recent advances in fluorescence in situ hybridization (FISH) in hematology.
    Berger R
    Pathol Biol (Paris); 1995 Mar; 43(3):175-80. PubMed ID: 7675544
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Comet-FISH using peptide nucleic acid probes detects telomeric repeats in DNA damaged by bleomycin and mitomycin C proportional to general DNA damage.
    Arutyunyan R; Gebhart E; Hovhannisyan G; Greulich KO; Rapp A
    Mutagenesis; 2004 Sep; 19(5):403-8. PubMed ID: 15388814
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Submicroscopic terminal deletions and duplications in retarded patients with unclassified malformation syndromes.
    Riegel M; Baumer A; Jamar M; Delbecque K; Herens C; Verloes A; Schinzel A
    Hum Genet; 2001 Sep; 109(3):286-94. PubMed ID: 11702209
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Study of 30 patients with unexplained developmental delay and dysmorphic features or congenital abnormalities using conventional cytogenetics and multiplex FISH telomere (M-TEL) integrity assay.
    Popp S; Schulze B; Granzow M; Keller M; Holtgreve-Grez H; Schoell B; Brough M; Hager HD; Tariverdian G; Brown J; Kearney L; Jauch A
    Hum Genet; 2002 Jul; 111(1):31-9. PubMed ID: 12136233
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Clinical applications of two-color telomeric fluorescence in situ hybridization for prenatal diagnosis: identification of chromosomal translocation in five families with recurrent miscarriages or a child with multiple congenital anomalies.
    Wakui K; Tanemura M; Suzumori K; Hidaka E; Ishikawa M; Kubota T; Fukushima Y
    J Hum Genet; 1999; 44(2):85-90. PubMed ID: 10083730
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Cryptic telomere imbalance: a 15-year update.
    Ledbetter DH; Martin CL
    Am J Med Genet C Semin Med Genet; 2007 Nov; 145C(4):327-34. PubMed ID: 17910073
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Sequential fluorescence in situ hybridization analysis for trisomy 12 in B-cell chronic lymphocytic leukemia.
    Hjalmar V
    Methods Mol Med; 2005; 115():231-40. PubMed ID: 15998971
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Comparative genomic hybridization: technical development and cytogenetic aspects for routine use in clinical laboratories.
    Lapierre JM; Cacheux V; Da Silva F; Collot N; Hervy N; Wiss J; Tachdjian G
    Ann Genet; 1998; 41(1):56-62. PubMed ID: 9599653
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Fluorescence in situ hybridization (FISH) in cytogenetics of leukemia.
    Michalová K
    Folia Biol (Praha); 1996; 42(6):311-4. PubMed ID: 9158941
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Submicroscopic unbalanced translocation resulting in del10p/dup13q detected by subtelomere FISH.
    Roos A; Rudnik-Schöneborn S; Eggermann K; Eggermann T; Senderek J; Schwanitz G; Zerres K; Schüler HM
    Eur J Med Genet; 2006; 49(6):505-10. PubMed ID: 16905374
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Rapid detection of subtelomeric deletion/duplication by novel real-time quantitative PCR using SYBR-green dye.
    Boehm D; Herold S; Kuechler A; Liehr T; Laccone F
    Hum Mutat; 2004 Apr; 23(4):368-78. PubMed ID: 15024731
    [TBL] [Abstract][Full Text] [Related]  

  • 33. FISH screening for subtelomeric rearrangements in 219 patients with idiopathic mental retardation and normal karyotype.
    Baroncini A; Rivieri F; Capucci A; Croci G; Franchi F; Sensi A; Battaglia P; Aiello V; Calzolari E
    Eur J Med Genet; 2005; 48(4):388-96. PubMed ID: 16378923
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Detection of submicroscopic aberrations in patients with unexplained mental retardation by fluorescence in situ hybridization using multiple subtelomeric probes.
    Fan YS; Zhang Y; Speevak M; Farrell S; Jung JH; Siu VM
    Genet Med; 2001; 3(6):416-21. PubMed ID: 11715006
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Identification of a subtle t(16;19)(p13.3;p13.3) in an infant with multiple congenital abnormalities using a 12-colour multiplex FISH telomere assay, M-TEL.
    Brown J; Horsley SW; Jung C; Saracoglu K; Janssen B; Brough M; Daschner M; Beedgen B; Kerkhoffs G; Eils R; Harris PC; Jauch A; Kearney L
    Eur J Hum Genet; 2000 Dec; 8(12):903-10. PubMed ID: 11175277
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Cytogenetics and fluorescence in-situ hybridization in detection of hematological malignancies.
    Frenny VJ; Antonella Z; Luisa A; Shah AD; Sheth JJ; Rocchi M
    Indian J Cancer; 2003; 40(4):135-9. PubMed ID: 14716109
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Detection of cryptic subtelomeric chromosome abnormalities and identification of anonymous chromatin using a quantitative multiplex ligation-dependent probe amplification (MLPA) assay.
    Northrop EL; Ren H; Bruno DL; McGhie JD; Coffa J; Schouten J; Choo KH; Slater HR
    Hum Mutat; 2005 Nov; 26(5):477-86. PubMed ID: 16170807
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Prenatal exclusion of subtelomeric deletion 1p by fluorescent in situ hybridization.
    Phupong V; Praphanphoj V; Shotelersuk V
    Arch Gynecol Obstet; 2007 Apr; 275(4):237-40. PubMed ID: 16983561
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Spectral karyotyping analysis of head and neck squamous cell carcinoma.
    Singh B; Gogineni S; Goberdhan A; Sacks P; Shaha A; Shah J; Rao P
    Laryngoscope; 2001 Sep; 111(9):1545-50. PubMed ID: 11568603
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Fluorescence in situ hybridization using the subtelomeric 11q probe as a diagnostic tool for congenital thrombocytopenia.
    Göhring G; Hanke C; Kratz C; Kontny U; Steinemann D; Niemeyer CM; Schlegelberger B
    Ann Hematol; 2006 Dec; 85(12):883-5. PubMed ID: 16977432
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.